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10338-85-9

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10338-85-9 Usage

General Description

2,2-dimethyl-6-(trichloromethyl)tetrahydro-4H-pyran-4-one is a chemical compound with a complex structure. It contains a tetrahydro-4H-pyran-4-one ring with a trichloromethyl group attached at the 6th carbon position and two methyl groups at the 2nd carbon position. 2,2-dimethyl-6-(trichloromethyl)tetrahydro-4H-pyran-4-one is commonly used as an intermediate in organic synthesis and can also act as a chiral building block in the production of pharmaceuticals and agrochemicals. It has been reported to have insecticidal and fungicidal properties, and is sometimes used as a pesticide. Additionally, it has potential applications in the development of new materials and chemical processes.ой

Check Digit Verification of cas no

The CAS Registry Mumber 10338-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,3 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10338-85:
(7*1)+(6*0)+(5*3)+(4*3)+(3*8)+(2*8)+(1*5)=79
79 % 10 = 9
So 10338-85-9 is a valid CAS Registry Number.

10338-85-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-6-(trichloromethyl)oxan-4-one

1.2 Other means of identification

Product number -
Other names 6-trichloromethyl-2,2-dimethyloxacyclohexan-4-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10338-85-9 SDS

10338-85-9Downstream Products

10338-85-9Relevant articles and documents

Lewis Acid Catalysis of Ene Addition of Chloral and Bromal to Olefins; Product Studies

Benner, Jill P.,Gill, G. Bryon,Parrott, Stephen J.,Wallace, Brian

, p. 291 - 313 (2007/10/02)

The addition of chloral and bromal to a variety of alkyl-substituted alkenes has been investigated.The effect of the reaction of varying the Lewis acid catalyst and the structure of substrate have been studied.Anhydrous AlCl3 was found to be most effective catalyst, and ene-type adducts were the major products in most cases.Side reactions were observed with the less reactive systems leading, variously, to the formation of trihalogenoketones, hydrohalogenated ene adducts, and cyclic ethers.Conditions for optimising the yield of ene adducts were established in some cases.The trihalogenoketone by-products can be conveniently removed by a Grignard-type reaction.

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